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Abstract Hepatic transcriptome and proteome responses against glutathione depletion were investigated by Affymetrix GeneChip Microarray and 2-dimensional gel electrophoresis (2D-DIGE), followed by MALDI-TOFMS analysis and utilizing a glutathione-depleted rat model treated with diethyl maleate (DEM)

have found that among the skeletal muscle biopsies of 28 ASD children with mitochondrial diseases, 50% had defects of complex I, 18% had combined defects of complex I and III, another 18% were identified with the combined defects of complexes I, III, and IV, and 14% were with defects of complex V [74]

Packaging : Available in 2mL ampoules and 10mL vials

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